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723449004: Pierson syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3424664019 Pierson syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424665018 Pierson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3424666017 Microcoria and congenital nephrosis syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403068016 A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403069012 A rare primary glomerular disease characterised by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pierson syndrome (disorder) Is a Congenital anomaly of eye true Inferred relationship Some
Pierson syndrome (disorder) Is a Congenital nephrotic syndrome false Inferred relationship Some
Pierson syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Pierson syndrome (disorder) Is a Steroid-resistant nephrotic syndrome true Inferred relationship Some
Pierson syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Pierson syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Pierson syndrome (disorder) Finding site Glomerulus structure true Inferred relationship Some 2
Pierson syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Pierson syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Pierson syndrome (disorder) Finding site Eye structure false Inferred relationship Some 2
Pierson syndrome (disorder) Finding site Glomerulus structure false Inferred relationship Some 3
Pierson syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Pierson syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Pierson syndrome (disorder) Finding site Eye structure true Inferred relationship Some 1
Pierson syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Pierson syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Pierson syndrome (disorder) Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Pierson syndrome (disorder) Interprets Albumin measurement true Inferred relationship Some 4
Pierson syndrome (disorder) Has interpretation Below reference range true Inferred relationship Some 4
Pierson syndrome (disorder) Interprets Measurement of protein in urine (procedure) true Inferred relationship Some 3
Pierson syndrome (disorder) Has interpretation Above reference range true Inferred relationship Some 3
Pierson syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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